Demographic, hemodynamic characteristics, and therapeutic trends of pulmonary hypertension patients: The Pulmonary Hypertension Mexican registry (REMEHIP).

IF 2.2 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pulmonary Circulation Pub Date : 2024-06-17 eCollection Date: 2024-04-01 DOI:10.1002/pul2.12395
Carlos Jerjes-Sánchez, Alicia Ramírez-Rivera, Nayeli Zayas Hernandez, Guillermo Cueto Robledo, Humberto García-Aguilar, Pedro Gutiérrez-Fajardo, Mario Seoane García de León, Francisco Moreno Hoyos-Abril, Miguel Ernesto Beltrán Gámez, Jose Elizalde, Tomás Pulido Fccp, Julio Sandoval
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Abstract

Data on demographic characteristics and therapeutic approaches in Latin American pulmonary arterial hypertension (PAH) patients are scarce. Pulmonary Hypertension Mexican registry (REMEHIP) is a multicenter Mexican registry of adult and pediatric patients, including prevalent and incident cases. Objective: assess clinical characteristics, treatment trends, and in-hospital outcomes. Inclusion: age >2 years, diagnosis of pulmonary hypertension (PH) (groups 1 and 4), right heart catheterization with mPAP ≥25 mmHg, PWP ≤ 15 mmHg, and PVR > 3 Wood unit (WU). We included 875 PH patients, 619 adults, 133 pediatric idiopathic PAH (IPAH), and 123 chronic thromboembolic pulmonary hypertension (CTEPH) patients. We enrolled 48.4% of the incident and 51.6% of the prevalent adult and pediatric patients. PAH adults: age 43 ± 15, females 81.9%, functional class (FC) (I/II) 66.5%, 6-min walk distance (6MWD) 378 ± 112 m, mPAP 57.3 ± 19.0 mmHg, confidence interval (CI) 3.3 ± 1.5 L/min/m2, PVR 12.0 ± 8.1 WU. PAH pediatrics: age 9 ± 5, females 51.1%, FC (I/II) 85.5%, 6MWD 376 ± 103 m, mPAP 49.7 ± 13.4 mmHg, CI 2.6 ± 0.9 L/min/m2, PVR 16.4 ± 13.5 WU. CTEPH: age 44 ± 17, females 56.1%, FC (I/II) 65.5%, 6MWD 369 ± 126 m, mPAP 49.7 ± 13.4 mmHg, CI 2.6 ± 0.9 L/min/m2, PVR 10.5 + 6.5 WU. When we analyzed the IPAH group separately, it sustained a high functional class I/II incidence. REMEHIP shows better functional class in young females with severe PAH than in American and European patients. Also, PAH pediatric patients had a better functional class than other registries. However, our registry also shows that our population's access to specific pharmacologic treatments is still far from optimal.

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肺动脉高压患者的人口统计学、血液动力学特征和治疗趋势:墨西哥肺动脉高压登记处(REMEHIP)。
有关拉丁美洲肺动脉高压(PAH)患者的人口特征和治疗方法的数据很少。墨西哥肺动脉高压登记处(REMEHIP)是墨西哥的一个多中心登记处,登记对象包括成人和儿童患者,包括流行病例和偶发病例。目的:评估临床特征、治疗趋势和院内预后。纳入条件:年龄大于 2 岁,诊断为肺动脉高压(PH)(第 1 组和第 4 组),右心导管检查结果为 mPAP ≥25 mmHg、PWP ≤ 15 mmHg 和 PVR > 3 Wood 单位(WU)。我们共纳入了 875 名 PH 患者,其中包括 619 名成人、133 名小儿特发性 PAH (IPAH) 和 123 名慢性血栓栓塞性肺动脉高压 (CTEPH) 患者。我们收治了 48.4% 的成人和儿童患者,以及 51.6% 的成人和儿童患者。PAH 成人:年龄 43 ± 15 岁,女性 81.9%,功能分级(FC)(I/II)66.5%,6 分钟步行距离(6MWD)378 ± 112 米,mPAP 57.3 ± 19.0 mmHg,置信区间(CI)3.3 ± 1.5 L/min/m2,PVR 12.0 ± 8.1 WU。PAH 儿科:年龄 9 ± 5 岁,女性 51.1%,FC(I/II)85.5%,6MWD 376 ± 103 m,mPAP 49.7 ± 13.4 mmHg,CI 2.6 ± 0.9 L/min/m2,PVR 16.4 ± 13.5 WU。CTEPH:年龄 44 ± 17 岁,女性 56.1%,FC(I/II)65.5%,6MWD 369 ± 126 米,mPAP 49.7 ± 13.4 mmHg,CI 2.6 ± 0.9 L/min/m2,PVR 10.5 + 6.5 WU。当我们单独分析 IPAH 组时,其功能分级 I/II 级的发生率较高。REMEHIP显示,年轻女性重度PAH患者的功能分级优于欧美患者。此外,PAH 儿科患者的功能分级也优于其他登记。不过,我们的登记也显示,我们的人群获得特殊药物治疗的机会还远远不够。
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来源期刊
Pulmonary Circulation
Pulmonary Circulation Medicine-Pulmonary and Respiratory Medicine
CiteScore
4.20
自引率
11.50%
发文量
153
审稿时长
15 weeks
期刊介绍: Pulmonary Circulation''s main goal is to encourage basic, translational, and clinical research by investigators, physician-scientists, and clinicans, in the hope of increasing survival rates for pulmonary hypertension and other pulmonary vascular diseases worldwide, and developing new therapeutic approaches for the diseases. Freely available online, Pulmonary Circulation allows diverse knowledge of research, techniques, and case studies to reach a wide readership of specialists in order to improve patient care and treatment outcomes.
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